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Perspectives on healthcare AI and product engineering.

Practical writing on building secure, useful digital products for regulated healthcare environments.

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Showing 25–33 of 33

Clinical Data ManagementPharma

Twelve questions that separate EDC vendors, none of them about price. What a good answer sounds like on…

Aug 16, 202610 min read

Clinical Data ManagementPharma

ePRO compliance rarely falls because patients lose interest. It falls because of the site workflow around it…

Aug 14, 20268 min read

Clinical Data ManagementPharma

Most SDTM pain starts in the eCRF, not the mapping spec. The CDASH design decisions that make submission…

Aug 12, 202610 min read

Clinical Data ManagementPharma

Query volume rarely spikes because sites got worse. It spikes because edit checks were written for the…

Aug 10, 20268 min read

AI in Life SciencesPharma

How agentic AI moves pharma and MedTech from assistants that answer to agents that execute, across…

Aug 10, 20264 min read

Clinical Data ManagementPharma

Two new fields, four systems and a training deck to reconcile. How to scope revalidation for a mid-study…

Aug 8, 20269 min read

Clinical Data ManagementPharma

eCRF design, edit checks, UAT, validation documentation and go-live: the real sequence of an EDC database…

Aug 6, 20269 min read

Clinical Data ManagementPharma

An EDC captures and validates trial data. It does not own your metadata, your export spec, your validation…

Aug 4, 20268 min read

Clinical OperationsClinical Research

Paper CRFs, scattered data, slow queries and delayed publications: five signs a clinical research workflow is…

Aug 3, 20264 min read